43742-2238 NDC - FNG (ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALTERNARIA TENUIS NEES, ASPERGILLUS NIGER, BERBERIS VULGARIS, BRUGIA MALAYI, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, CARBOLICUM ACIDUM, COCHLEARIA ARMORACIA, ECHINACEA (ANGUSTIFOLIA), FERRUM METALLICUM, FORMALINUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, IRIDIUM METALLICUM, LOMATIUM DISSECTUM, LYCOPODIUM CLAVATUM, METHYLCOBALAMIN, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH), MYRRHA, PHOSPHORICUM ACIDUM, PROPOLIS, PULSATILLA (PRATENSIS), RHIZOPUS NIGRICANS,)

Drug Information

  • Product NDC: 43742-2238
  • Proprietary Name: FNG
  • Non Proprietary Name: Adenosinum Triphosphoricum Dinatrum, Alternaria Tenuis Nees, Aspergillus Niger, Berberis Vulgaris, Brugia Malayi, Candida Albicans, Candida Parapsilosis, Carbolicum Acidum, Cochlearia Armoracia, Echinacea (Angustifolia), Ferrum Metallicum, Formalinum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Iridium Metallicum, Lomatium Dissectum, Lycopodium Clavatum, Methylcobalamin, Mucor Racemosus, Mutabile Bacillus (Bach), Myrrha, Phosphoricum Acidum, Propolis, Pulsatilla (Pratensis), Rhizopus Nigricans,
  • Active Ingredient(s): 12 [hp_X]/mL ADENOSINE TRIPHOSPHATE DISODIUM; 64 [hp_X]/mL ALTERNARIA ALTERNATA; 16 [hp_X]/mL ASPERGILLUS NIGER VAR. NIGER; 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK; 39 [hp_C]/mL BRUGIA MALAYI; 12 [hp_X]/mL CANDIDA ALBICANS; 12 [hp_X]/mL CANDIDA PARAPSILOSIS; 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 30 [hp_C]/mL ESCHERICHIA COLI; 8 [hp_X]/mL FORMALDEHYDE SOLUTION; 6 [hp_X]/mL GOLDENSEAL; 3 [hp_X]/mL HORSERADISH; 12 [hp_X]/mL IRIDIUM; 12 [hp_X]/mL IRON; 12 [hp_X]/mL LACTIC ACID, L-; 3 [hp_X]/mL LOMATIUM DISSECTUM ROOT; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 12 [hp_X]/mL METHYLCOBALAMIN; 16 [hp_X]/mL MUCOR RACEMOSUS; 3 [hp_X]/mL MYRRH; 12 [hp_X]/mL PHENOL; 12 [hp_X]/mL PHOSPHORIC ACID; 6 [hp_X]/mL PROPOLIS WAX; 12 [hp_X]/mL PULSATILLA PRATENSIS WHOLE; 14 [hp_C]/mL RHIZOPUS STOLONIFER; 12 [hp_X]/mL SACCHAROMYCES CEREVISIAE; 12 [hp_X]/mL SELENIUM; 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND; 8 [hp_X]/mL SUS SCROFA THYMUS; 8 [hp_X]/mL TABEBUIA IMPETIGINOSA BARK; 12 [hp_X]/mL ZINC
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Food Additives [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/20/2024

Package Information

No. Package Code Package Description Billing Unit
143742-2238-130 mL in 1 BOTTLE, DROPPER (43742-2238-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2238The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEFNGThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAdenosinum Triphosphoricum Dinatrum, Alternaria Tenuis Nees, Aspergillus Niger, Berberis Vulgaris, Brugia Malayi, Candida Albicans, Candida Parapsilosis, Carbolicum Acidum, Cochlearia Armoracia, Echinacea (Angustifolia), Ferrum Metallicum, Formalinum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Iridium Metallicum, Lomatium Dissectum, Lycopodium Clavatum, Methylcobalamin, Mucor Racemosus, Mutabile Bacillus (Bach), Myrrha, Phosphoricum Acidum, Propolis, Pulsatilla (Pratensis), Rhizopus Nigricans,The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/20/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEADENOSINE TRIPHOSPHATE DISODIUM; ALTERNARIA ALTERNATA; ASPERGILLUS NIGER VAR. NIGER; BERBERIS VULGARIS ROOT BARK; BRUGIA MALAYI; CANDIDA ALBICANS; CANDIDA PARAPSILOSIS; ECHINACEA ANGUSTIFOLIA WHOLE; ESCHERICHIA COLI; FORMALDEHYDE SOLUTION; GOLDENSEAL; HORSERADISH; IRIDIUM; IRON; LACTIC ACID, L-; LOMATIUM DISSECTUM ROOT; LYCOPODIUM CLAVATUM SPORE; METHYLCOBALAMIN; MUCOR RACEMOSUS; MYRRH; PHENOL; PHOSPHORIC ACID; PROPOLIS WAX; PULSATILLA PRATENSIS WHOLE; RHIZOPUS STOLONIFER; SACCHAROMYCES CEREVISIAE; SELENIUM; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; TABEBUIA IMPETIGINOSA BARK; ZINCAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 64; 16; 3; 39; 12; 12; 3; 30; 8; 6; 3; 12; 12; 12; 3; 12; 12; 16; 3; 12; 12; 6; 12; 14; 12; 12; 8; 8; 8; 12 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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This page was last updated on: 6/6/2025

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